CAS: 79-05-0; Propionamide

该化合物是一种单纯的脂酰胺,来自丙酸,其特点是水和极有机溶剂中白色晶状固体形式和溶解性,是有机合成的多功能中间体,特别是在生产药品,农用化学品和特殊化学品方面.其薄膜功能组有助于水解,减少和凝聚等反应.Propionamide还被用作研究氨化物结合行为和分子相互作用的模型化合物.关键优势包括其在标准条件下的稳定性,合成应用的高纯度和与一系列工业工艺的兼容性.

结构式图片

相似化合物

556-53-6 4905-83-3 14488-45-0

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

diazoacetone 1-thiopropane propene propyl sulfideN-xanthen-9-yl-propionamideN-xanthen-9-yl-propionamide N-(2-[4]pyridyl-ethyl)-propionamideN-(2-[4]pyridyl-ethyl)-propionamide quinazoline6-ethylbenzimidazo1,2-cquinazoline Hexahydro-1,3,5-trinitro-1,3,5-triazine

合成工艺路线路线简述

  • 合成目标产物 Propionamide 主要起始原料 Propionyl Chloride
  • 79-06-1 = 79-05-0
    反应条件:1.1 Reagents: Hydrogen Catalysts: Nickel Boride (Resin Bound) Solvents: Methanol
    标题:An Excellent Nickel Boride Catalyst For The Selective Hydrogenation Of Olefins
    作者:Choi,Jaesung; Yoon,Nung Min
    参考文献:Synthesis 日期:1996 卷标:(5) 页码:597-599]

    = 79-05-0
    反应条件:1.1 Reagents: Sodium Bicarbonate,Hydroxyamine Hydrochloride Catalysts: 2761983-03-1 Solvents: Water; 2 H,313 K
    标题:Mechanochemical Synthesis Of Half-Sandwich Iridium/rhodium Complexes With 8-Hydroxyquinoline Derivatives Ligands
    作者:Jia,Wei-Guo; Li,Xiao-Dong; Zhi,Xue-Ting; Zhong,Rui
    参考文献:Applied Organometallic Chemistry 日期:2022 卷标:36(4)]

    79-06-1 = 79-05-0
    反应条件:1.1 Reagents: Hydrogen Catalysts: Phosphine,Tris(4-Ethenylphenyl)-,Polymer With 1,3,5-Tribromobenzene (Post-Treated With Pd Nanoparticles) Solvents: Ethanol; 1 H,1 Atm,Rt
    标题:Palladium/phosphorus-Doped Porous Organic Polymer As Recyclable Chemoselective And Efficient Hydrogenation Catalyst Under Ambient Conditions
    作者:Ding,Zong-Cang; Li,Cun-Yao; Chen,Jun-Jia; Zeng,Jia-Hao; Tang,Hai-Tao; Et Al
    参考文献:Advanced Synthesis & Catalysis 日期:2017 卷标:359(13) 页码:2280-2287]

    = 79-05-0
    反应条件:1.1 Reagents: Water Catalysts: [2,6-Bis(Diphenylmethyl)-4-Methylbenzenamine]Dichloro[(1,2,3,4,5,6-η)-1-Methyl-4...; 4 H,Rt
    标题:Water-Soluble Superbulky (η6-P-Cymene) Ruthenium(Ii) Amine: An Active Catalyst In The Oxidative Homocoupling Of Arylboronic Acids And The Hydration Of Organonitriles
    作者:Nirmala,Muthukumaran; Adinarayana,Mannem; Ramesh,Karupnaswamy; Maruthupandi,Mannarsamy; Vaddamanu,Moulali; Et Al
    参考文献:New Journal Of Chemistry 日期:2018 卷标:42(18) 页码:15221-15230]

    79-06-1 = 79-05-0
    反应条件:1.1 Reagents: Formic Acid Catalysts: Palladium Diacetate,1,1′-(9,9-Dimethyl-9H-Xanthene-4,5-Diyl)Bis[1,1-Diphenylphosphine] Solvents: Water; 20 H,90 °C
    标题:Facile Pd-Catalyzed Chemoselective Transfer Hydrogenation Of Olefins Using Formic Acid In Water
    作者:Liu,Tianxiang; Zeng,Yongming; Zhang,Hongxi; Wei,Ting; Wu,Xia; Et Al
    参考文献:Tetrahedron Letters 日期:2016 卷标:57(43) 页码:4845-4849]

    79-06-1 = 79-05-0
    反应条件:1.1 Reagents: Ammonium Formate Catalysts: Ruthenium(1+),Bis(Acetonitrile)(η5-2,4-Cyclopentadien-1-Yl)[tris(1-Methylethyl)... Solvents: Methanol; 4 H,60 °C
    标题:Transfer Hydrogenation Of Unsaturated Substrates By Half-Sandwich Ruthenium Catalysts Using Ammonium Formate As Reducing Reagent
    作者:Mai,Van Hung; Lee,San-Hwa; Nikonov,Georgii I.
    参考文献:Chemistryselect 日期:2017 卷标:2(25) 页码:7751-7757]

    79-06-1 = 79-05-0
    反应条件:1.1 Reagents: Formic Acid Catalysts: Palladium (Supported On Fibrous-Structured Silica Nanospheres) Solvents: Methanol,Water; 12 H,100 °C
    标题:Palladium Nanoparticles Supported On Fibrous-Structured Silica Nanospheres (Kcc-1): An Efficient And Selective Catalyst For The Transfer Hydrogenation Of Alkenes
    作者:Qureshi,Ziyauddin S.; Sarawade,Pradip B.; Albert,Matthias; D'Elia,Valerio; Hedhili,Mohamed N.; Et Al
    参考文献:Chemcatchem 日期:2015 卷标:7(4) 页码:635-642]

    = 79-05-0
    反应条件:1.1 Reagents: Aldoxime Catalysts: Cupric Chloride Solvents: Methanol; 4 H,65 °C
    标题:A Heterogeneous Catalytic Method For The Conversion Of Nitriles Into Amides Using Molecular Sieves Modified With Copper(Ii)
    作者:Kiss,Arpad; Hell,Zoltan
    参考文献:Tetrahedron Letters 日期:2011 卷标:52(45) 页码:6021-6023]

    79-06-1 = 79-05-0
    反应条件:1.1 Reagents: Hydrogen Catalysts: Palladium,Dichloro[1-[(Dimethylamino)Methyl]-2-[(4-Methylphenyl)Thio]Ferrocene-... Solvents: Acetone
    标题:Application Of Palladium Ferrocenyl Amine Sulfide Complexes In The Hydrogenation Of Carbon-Carbon Double And Triple Bonds
    作者:Ali,Hussein M.; Naiini,Ahmad A.; Brubaker,Carl H. Jr.
    参考文献:Journal Of Molecular Catalysis 日期:1992 卷标:77(2) 页码:125-34]

    79-06-1 = 79-05-0
    反应条件:1.1 Reagents: Hydrogen Solvents: Ethanol; 1 H,2 Mpa,100 °C
    标题:Reactivity And Mechanism Investigation Of Selective Hydrogenation Of 2,3,5-Trimethylbenzoquinone On In Situ Generated Metallic Cobalt
    作者:Su,Diefeng; Wei,Zhongzhe; Mao,Shanjun; Wang,Jing; Li,Yi; Et Al
    参考文献:Catalysis Science & Technology 日期:2016 卷标:6(12) 页码:4503-4510]

    79-06-1 = 79-05-0
    反应条件:1.1 Reagents: Hydrogen Catalysts: Palladium,Carbon Solvents: Ethanol; 0.5 H,1 Bar,30 °C
    标题:Highly Efficient And Chemoselective Hydrogenation Of α,β-Unsaturated Carbonyls Over Pd/n-Doped Hierarchically Porous Carbon
    作者:Wei,Zhongzhe; Gong,Yutong; Xiong,Tianyi; Zhang,Pengfei; Li,Haoran; Et Al
    参考文献:Catalysis Science & Technology 日期:2015 卷标:5(1) 页码:397-404]

    = 79-05-0
    反应条件:1.1 Catalysts: Manganese Oxide (Mno2) Solvents: Water; 15 Min,100 Psi,70 °C
    标题:Mild And Selective Heterogeneous Catalytic Hydration Of Nitriles To Amides By Flowing Through Manganese Dioxide
    作者:Battilocchio,Claudio; Hawkins,Joel M.; Ley,Steven V.
    参考文献:Organic Letters 日期:2014 卷标:16(4) 页码:1060-1063]

    79-06-1 = 79-05-0
    反应条件:1.1 Reagents: Hydrogen Solvents: Methanol; 29 Bar,30 °C
    标题:Large Centimeter-Sized Macroporous Ferritin Gels As Versatile Nanoreactors
    作者:Kumari,Sushma; Kulkarni,Amol; Kumaraswamy,Guruswamy; Sen Gupta,Sayam
    参考文献:Chemistry Of Materials 日期:2013 卷标:25(23) 页码:4813-4819]

    = 79-05-0
    反应条件:1.1 Catalysts: Ruthenium(1+),Dichloro[(1,2,3,4,5,6-η)-1-Methyl-4-(1-Methylethyl)Benzene][1-[3-... (Supported On Silica-Coated Nanoferrite) Solvents: Water; 2 H,100 - 120 Psi,150 °C
    标题:Chemistry By Nanocatalysis: First Example Of A Solid-Supported Rapta Complex For Organic Reactions In Aqueous Medium
    作者:Garcia-Garrido,Sergio E.; Francos,Javier; Cadierno,Victorio; Basset,Jean-Marie; Polshettiwar,Vivek
    参考文献:Chemsuschem 日期:2011 卷标:4(1) 页码:104-111]

    = 79-05-0
    反应条件:1.1 Reagents: Niobium Pentachloride Solvents: Dichloromethane; Rt1.2 Reagents: Ammonia; 0.5 H,Rt; Rt -> 50 °C; 1 H,40 - 50 °C
    标题:Niobium Pentachloride Promoted Conversion Of Carboxylic Acids To Carboxamides: Synthesis Of The 4-Aryl-1,2,3,4-Tetrahydroisoquinoline Alkaloid Structures
    作者:Nery,Marcelo S.; Ribeiro,Renata P.; Lopes,Claudio C.; Lopes,Rosangela S. C.
    参考文献:Synthesis 日期:2003 卷标:(2) 页码:272-276]

    = 79-05-0
    反应条件:1.1 Reagents: Potassium Bicarbonate,Hydroxyamine Hydrochloride Catalysts: Cobalt Oxide (Co3O4),Copper Solvents: Acetonitrile,Water; 1 Mpa,Rt; 6 H,140 °C
    标题:Kinetic Analysis Of Consecutive/parallel Transformation Of Furfural To Biomass-Based Primary Amide By Using A "Concentration-Time" Integral
    作者:Yang,Shengwen; Chen,Jinzhu
    参考文献:Acs Catalysis 日期:2023 卷标:13(1) 页码:113-131]

    79-06-1 = 79-05-0
    反应条件:1.1 Reagents: Sodium Borohydride Catalysts: Cuprous Chloride Solvents: Ethanol; Rt; 30 H,Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; Ph 5 - 6,Rt
    标题:Selective Reduction Of α,β-Unsaturated Amides With Nabh4-Cucl/etoh
    作者:Li,Jian-Ping; Zhang,Yong-Xia; Su,Ling-Yun; Meng,Ge; Guo,Hai-Ming
    参考文献:Henan Shifan Daxue Xuebao 日期:2012 卷标:40(2) 页码:101-103]

    120157-99-5 = 79-05-0
    反应条件:1.1 Reagents: Trifluoroacetic Acid Solvents: Dichloromethane
    标题:A New Method For The Synthesis Of Amides From Amines: Ruthenium Tetroxide Oxidation Of N-Protected Alkylamines
    作者:Tanaka,Kenichi; Yoshifuji,Shigeyuki; Nitta,Yoshihiro
    参考文献:Chemical & Pharmaceutical Bulletin 日期:1988 卷标:36(8) 页码:3125-9]

    = 79-05-0
    反应条件:1.1 Catalysts: Tricyclohexylphosphine,Bis[(1,2,5,6-η)-1,5-Cyclooctadiene]Di-μ-Methoxydirhodium Solvents: Toluene,Tetrahydrofuran; 15 Min,25 °C1.2 Solvents: Isopropanol,Water; 24 H,25 °C
    标题:Rhi-Catalyzed Hydration Of Organonitriles Under Ambient Conditions
    作者:Goto,Akihiro; Endo,Kohei; Saito,Susumu
    参考文献:Angewandte Chemie 日期:2008 卷标:47(19) 页码:3607-3609
丙腈置于水体系中,化学反应 36.0H,以55%的收率获得产物丙酰胺
参考文献:几丁质负载钌催化剂将腈水合为酰胺†
标题:几丁质负载钌催化剂将腈水合为酰胺†
摘要:几丁质负载的钌(ru /几丁质)在水性条件下促进腈水合成羧酰胺.腈水合可以以克为单位进行,并且与各种官能团的存在相容,所述官能团包括烯烃,醛,羧酸酯以及硝基和苄氧基羰基.钌/几丁质催化剂可以容易地由可商购的几丁质,氯化钌(iii)和硼氢化钠制备.通过高分辨率透射电子显微镜对钌/甲壳质的分析表明,甲壳素载体上存在钌纳米颗粒.
DOI:10.1039/c4Ra15682J

海关参考信息

专利信息


专利号:US-11548898-B2
优先权日:2017-07-06
标题 :Synthesis of halichondrins
发明人:KISHI YOSHITO; AI YANRAN; YE NING; WANG QIAOYI; YAHATA KENZO; ISO Kentaro; NAINI SANTHOSH REDDY; YAMASHITA SHUJI; LEE JIHOON; OHASHI ISAO; FUKUYAMA TAKASHI
权利人:HARVARD COLLEGE; EISAI R&D MAN CO LTD
摘要:The present invention provides methods for the synthesis of ketones involving a Ni/Zr-mediated coupling reaction. The Ni/Zr-mediated ketolization reactions can be used in the synthesis of halichondrins (e.g., halichondrin A, B, C; homohalichondrin A, B, C; norhalichondrin A, B, C), and analogs thereof. Therefore, the present invention also provides synthetic methods useful for the synthesis of halichondrins, and analogs thereof. Also provided herein are compounds (i.e., intermediates) useful in the synthesis of halichondrins, and analogs thereof. In particular, the present invention provides methods and compounds useful in the synthesis of compound of Formula (H3-A).

专利号:US-2004058888-A1
优先权日:2000-01-13
标题:Methods for synthesis of alpha-d-gal (1~>3) gal-containing oligosaccharides
发明人:BORNAGHI LAURENT; DEKANY GYULA; DRINNAN NICHOLAS BARRY; PAPAGEORGIOU JOHN; WEST MICHAEL LEO
摘要:This invention relates to reagents and methods for synthesis of biologically active di- and tri-saccharides comprising α-D-Gal(1→3)-D-Gal. In particular the invention provides novel reagents, intermediates and processes for the solution or solid phase synthesis of α-D-galactopyranosyl-(1→3)-D-galactose, and derivatives thereof. In one preferred embodiments the invention provides a protected monosaccharide building block of general formula (II): in which R 3 is methoxy or methyl; R 1 is H, benzoyl, pivaloyl, 4-chlorobenzoyl, acetyl, chloroacetyl, levulinoyl, 4-methylbenzoyl, benzyl, 3,4-methylenedioxybenzyl, 4-methoxybenzyl, 4-chlorobenzyl, 4-acetamidobenzyl, or 4-azidobenzyl; and R 2 is H, Fmoc, benzoyl, pivaloyl, 4-chlorobenzoyl, acetyl, chloroacetyl, levulinoyl, 4-methylbenzoyl, benzyl, 3,4-methylenedioxybenzyl, 4-methoxybenzyl, 4 -chlorobenzyl, 4-acetamidobenzyl, or 4-azidobenzyl.

专利号:US-7326805-B2
优先权日:2003-05-07
标题 :Method for the synthesis of 4-hydroxyisoleucine and the derivatives thereof
发明人:MIOSKOWSKI CHARLES; CATALA CEDRIC; WAGNER ALAIN
权利人:MIOSKOWSKI CHARLES; CATALA CEDRIC; WAGNER ALAIN
摘要:The invention relates to a method for the synthesis of two isomers, at function OH, alone or in mixtures, of amino acids α or the derivatives thereof, having general formula (B), wherein: linkage C—O of the 4-position carbon (represented by symbol) denotes one or other of isomers III or IV, or mixtures thereof. Moreover, R 1 and R 2 represent: a hydrogen atom; or either R 1 or R 2 represents a hydrogen atom and the other substituent is a radical R a , an acyl group —COR a , such as acetyl, or a functional group —COOR a , —SO 2 R a , —N (R a , R b ), R a and R b , which are identical or different, representing a C1-C12 linear or branched alkyl radical, optionally substituted, an aryl group with one or more aromatic rings and heterocycles, comprising between 5 and 8C, optionally substituted, or aralkyl, the alkyl substituent and the aryl group being as defined above; or R 1 and R 2 both represent a substituent as defined above. R 3 represents a hydrogen atom or R a and R 4 has the significance of R a . The invention is characterised in that it comprises: the isomerisation of a compound having formula (I), wherein R 1 , R 2 , R a , R 3 and R 4 are as defined above, such as to produce a compound having formula (II); and the reduction of the carbonyl function thereof which, depending on the catalytic system employed and the formula (I) compound used, produces one of the isomers having general formula (III) or (IV) or a mixture thereof having formula (B). The invention can be used for the synthesis of (2S, 3R, 4S)-4-hydroxyisoleucine.

专利号:US-2012165520-A1
优先权日:2010-12-23
标题:Process for the synthesis of prodrugs of opioids
发明人:MCGEE PAUL; GARNETT IAN; JUAN E; MANAGE A; CARNIAUX JEAN-FRANCOIS
权利人:MCGEE PAUL; GARNETT IAN; JUAN E; MANAGE A; CARNIAUX JEAN-FRANCOIS
摘要:The present invention provides a process for the synthesis of opioid prodrugs. In particular, the present invention provides a process for the synthesis of opioid prodrugs comprising: treating an opioid, in the form of a salt or a freebase, with a carbonyl synthon to form an activated intermediate and subsequently reacting the activated intermediate with an amine, in the form of a salt or a freebase.

专利号:WO-2021035382-A1
优先权日:2019-08-23
标题:Method forcontinuous synthesis of 2-cyclopentene-1-one
发明人:HONG HAO; LU JIANGPING; BAO DENGHUI; YUAN LONG; WANG BO
权利人:LIAONING ASYMCHEM LABORATORIES CO LTD
摘要:Provided is a method for the continuous synthesis of 2-cyclopenten-1-one. The continuous synthesis method comprises: loading a catalyst in a continuous reaction device, then continuously conveying cyclopentene, an oxidant and a solvent into the continuous reaction device for an oxidation reaction, and continuously discharging 2-cyclopentene-1-one. In the presence of the catalyst and the solvent, cyclopentene is used as a starting material, and same is directly oxidized by the oxidant, which can avoid the generation of a large amount of halogen-containing three wastes; at the same time, the entire continuous synthesis process is carried out in the continuous reaction device, which can effectively inhibit the occurrence of safety risks during scale-up production; in addition, after the reaction is complete, the product system of the oxidation reaction can be simply concentrated to obtain the target product (2-cyclopenten-1-one). Thus, the purity (up to 98% and above) and separation rate (up to 79%) of the product are greatly improved, and production can be easily scaled up.

专利号:US-2024228455-A1
优先权日:2021-04-27
标 题 :Synthesis of cbn and cbnv
发明人:KAVARANA MALCOLM J
权利人:TEEWINOT LIFE SCIENCES CORP
摘要:The invention includes chemical synthesis for preparing cannabinol (CBN) and cannabinovarin (CBNV). The process is suitable for inter alia the large-scale synthesis of pharmaceutical grade CBN and CBNV.
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✅ COA系统入驻 | 共享模式

主要参考文献

[参考文献]: Anne Marie Hickey, Et Al. A Microreactor For The Study Of Biotransformations By A Cross-Linked Gamma-Lactamase Enzyme. Biotechnol J. 2009 Apr;4(4):510-6.
[参考文献]: Axel Rydevik, Et Al. Mass Spectrometric Characterization Of Glucuronides Formed By A New Concept, Combining Cunninghamella Elegans With Tempo. J Pharm Biomed Anal. 2013 Oct:84:278-84.
[参考文献]: Caiyue Liu, Et Al. The Effects Of Exercise On Synaptic Stripping Require Androgen Receptor Signaling. Plos One. 2014 Jun 2;9(6):E98633.
[参考文献]: Casey E Bohl, Et Al. Effect Of B-Ring Substitution Pattern On Binding Mode Of Propionamide Selective Androgen Receptor Modulators. Bioorg Med Chem Lett. 2008 Oct 15;18(20):5567-70.
[参考文献]: F Ros, Et Al. New Verapamil Related N-Homoveratryl Propionamides Which Sensitize Tumor Cells. Pharmazie. 1994 Oct;49(10):778-9.

合成参考文献


参考文献:10.1186/1297-9716-42-83
摘要:Barker EN, Darby AC, Helps CR, Peters IR, Heesom KJ, Arthur CJ, Crossett B, Hughes MA, Radford AD, Tasker S. Molecular characterization of the uncultivatable hemotropic bacterium Mycoplasma haemofelis. Veterinary Research. 2011 Jul 12;42(1):83. doi: 10.1186/1297-9716-42-83.
参考文献:10.1007/s00894-011-1166-5
摘要:Xiao X, Tan Y, Zhu L, Guo Y, Wen Z, Li M, Pu X, Tian A. Effects of the position and manner of hydration on the stability of solvated N-methylacetamides and the strength of binding between N-methylacetamide and water clusters: a computational study. Journal of Molecular Modeling. 2011 Jul 15;18(4):1389–99. doi: 10.1007/s00894-011-1166-5.
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